Baccinex
Adragos Pharma is a global Contract Development and Manufacturing Organization (CDMO) committed to providing comprehensive drug development and manufacturing services. With a customer-centric philosophy, they operate state-of-the-art facilities across Europe and Japan, specializing in small molecules, biologics, clinical trials, fill-and-finish, lyophilization, and sterile manufacturing. Their mission is to ensure high-quality, safe, and effective pharmaceutical products through innovative solutions, strict regulatory compliance, and a global network of facilities.
Industries
Nr. of Employees
small (1-50)
Products
High-throughput aseptic filling line (ampoules/vials)
Aseptic filling equipment with robotic handling, isolator/RABS integration, tool-less changeovers and filtration systems for high annual throughput across multiple container sizes.
High-throughput aseptic filling line (ampoules/vials)
Aseptic filling equipment with robotic handling, isolator/RABS integration, tool-less changeovers and filtration systems for high annual throughput across multiple container sizes.
Services
Integrated CDMO services
End-to-end services from early development to commercial manufacturing, including formulation, analytical development, regulatory support and supply chain management.
Clinical manufacturing and clinical supply
GMP clinical-material production including aseptic fill & finish, lyophilization and clinical kit preparation with clinical supply chain coordination.
Commercial manufacturing across multiple dosage forms
Large-scale production and packaging for sterile liquids, non-sterile liquids, semi-solids, oral solids and suppositories with quality and regulatory oversight.
Analytical development, validation and QC testing
Method development and validation, chromatographic and spectrophotometric assays, stability studies and routine release testing under GMP conditions.
Packaging, visual inspection and primary/secondary packaging
Primary and secondary packaging services with automated/semi-manual visual inspection to ensure container and product integrity prior to release.
R&D and small-scale GMP-like development (Athens site)
On-site R&D laboratory services for formulation, preformulation, analytical development and small-scale process development with capability to support HPAPI projects.
Integrated CDMO services
End-to-end services from early development to commercial manufacturing, including formulation, analytical development, regulatory support and supply chain management.
Clinical manufacturing and clinical supply
GMP clinical-material production including aseptic fill & finish, lyophilization and clinical kit preparation with clinical supply chain coordination.
Commercial manufacturing across multiple dosage forms
Large-scale production and packaging for sterile liquids, non-sterile liquids, semi-solids, oral solids and suppositories with quality and regulatory oversight.
Analytical development, validation and QC testing
Method development and validation, chromatographic and spectrophotometric assays, stability studies and routine release testing under GMP conditions.
Packaging, visual inspection and primary/secondary packaging
Primary and secondary packaging services with automated/semi-manual visual inspection to ensure container and product integrity prior to release.
R&D and small-scale GMP-like development (Athens site)
On-site R&D laboratory services for formulation, preformulation, analytical development and small-scale process development with capability to support HPAPI projects.
Expertise Areas
- Clinical trial manufacturing and clinical supply
- Biologics CMC and aseptic biopharmaceutical manufacturing
- Formulation and process development for small molecules and biologics
- Analytical method development, validation and stability testing
Key Technologies
- Aseptic filling systems (isolators and RABS)
- Blow–Fill–Seal (BFS) technology
- Lyophilization (freeze-drying)
- Robotic handling and automation for filling lines